# FDA Inspection 1107226 - Bausch & Lomb Inc - October 08, 2019

Source: https://www.keypedia.com/records/fda_inspections/bausch-lomb-inc/c3b0a67a-3a59-44be-8e03-0ef2b47eaab0
Source feed: FDA_Inspections

> FDA Inspection 1107226 for Bausch & Lomb Inc on October 08, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1107226
- Company Name: Bausch & Lomb Inc
- Inspection Date: 2019-10-08
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1107226 - 2019-10-08](https://www.keypedia.com/records/fda_inspections/bausch-lomb-inc/9386fbd5-d328-4230-aacc-8ce66162cbf8)
- [FDA Inspection 978030 - 2016-06-10](https://www.keypedia.com/records/fda_inspections/bausch-lomb-inc/5d56b0db-8ba2-4ba6-b971-b90f4de1324e)
- [FDA Inspection 978030 - 2016-06-10](https://www.keypedia.com/records/fda_inspections/bausch-lomb-inc/e6b707f0-594e-4de6-88ca-206f4902697f)
- [FDA Inspection 978030 - 2016-06-10](https://www.keypedia.com/records/fda_inspections/bausch-lomb-inc/42ebcf06-7707-48a0-9589-3ed17cb0f039)
- [FDA Inspection 826558 - 2013-03-15](https://www.keypedia.com/records/fda_inspections/bausch-lomb-inc/6f453e1f-b93a-428b-96bc-073150395e67)

Company: https://www.keypedia.com/companies/bausch-lomb-inc/6e2d24ec-25b4-419c-ba74-db88dd714834

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7